Canonical Allele Identifier: CA496764442

Gene: SLC38A8

Linked Data

• MyVariant Identifiers: chr16:g.84065543C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84031938C>T , CM000678.2:g.84031938C>T	GRCh38
NC_000016.9:g.84065543C>T , CM000678.1:g.84065543C>T	GRCh37
NC_000016.8:g.82623044C>T	NCBI36
NG_034136.1:g.15220G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.561G>A MANE Select	ENSP00000299709.3:p.Leu187=
ENST00000299709.7:c.561G>A	ENSP00000299709.3:p.Leu187=
ENST00000568178.1:c.561G>A	ENSP00000457737.1:p.Leu187=
NM_001080442.2:c.561G>A	NP_001073911.1:p.Leu187=
XM_011522872.1:c.561G>A	XP_011521174.1:p.Leu187=
XM_017022946.1:c.561G>A	XP_016878435.1:p.Leu187=
NM_001080442.3:c.561G>A MANE Select	NP_001073911.1:p.Leu187=